Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Glioblastoma
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Outcomes Assessor)Masking Description: Participants will be masked until postoperative period. Outcome assessor will be masked until all predefined outcomes have been analysedPrimary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 70 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04243005
Collaborators
  • Turku University Hospital
  • Odense University Hospital
  • Sahlgrenska University Hospital, Sweden
  • Karolinska University Hospital
  • Rikshospitalet University Hospital
  • Aarhus University Hospital
  • Norwegian University of Science and Technology
  • University Hospital of North Norway
  • Kuopio University Hospital
  • Tampere University Hospital
  • University Hospital, Linkoeping
  • Helsinki University Central Hospital
  • Uppsala University Hospital
  • University Hospital, Umeå
  • Skane University Hospital
  • Haukeland University Hospital
  • Ullevaal University Hospital
  • Rigshospitalet, Denmark
  • Oulu University Hospital
Investigators
Principal Investigator: Asgeir S Jakola, MD, PhD St.Olavs University Hospital and Sahlgrenska University Hospital Study Director: Geir Bråthen, MD, PhD St. Olavs Hospital